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Christopher M Grochowski

Showing results (1-10 of 72) with videos related to

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Genes|August 28, 2025
Structural Variants: Mechanisms, Mapping, and Interpretation in Human GeneticsShruti Pande, Moez Dawood, Christopher M Grochowski
Current Protocols|May 22, 2024
Validation of Single-Nucleotide Mosaic Variants Through Droplet Digital PCRChristopher M Grochowski, Richard A Gibbs, Harsha Doddapaneni
Gene|November 10, 2015
Jagged1 (JAG1): Structure, expression, and disease associationsChristopher M Grochowski, Kathleen M Loomes, Nancy B Spinner
Trends in Genetics : TIG|July 12, 2022
Complex genomic rearrangements: an underestimated cause of rare diseasesJakob Schuy, Christopher M Grochowski, Claudia M B Carvalho, et al.
Current Protocols in Human Genetics|March 17, 2020
Quantitative Assessment of Parental Somatic Mosaicism for Copy-Number Variant (CNV) DeletionsQian Liu, Christopher M Grochowski, Weimin Bi, et al.
Journal of Child and Adolescent Psychopharmacology|August 18, 2017
CHRNA7 Deletions are Enriched in Risperidone-Treated Children and AdolescentsMadelyn A Gillentine, Janson J White, Christopher M Grochowski, et al.
Biorxiv : the Preprint Server for Biology|February 14, 2024
Genome-wide maps of highly-similar intrachromosomal repeats that mediate ectopic recombination in three human genome assembliesLuis Fernandez-Luna, Carlos Aguilar-Perez, Christopher M Grochowski, et al.
HGG Advances|December 26, 2024
Genome-wide maps of highly-similar intrachromosomal repeats that can mediate ectopic recombination in three human genome assembliesLuis Fernandez-Luna, Carlos Aguilar-Perez, Christopher M Grochowski, et al.
Journal of Affective Disorders|July 21, 2018
CHRNA7 copy number gains are enriched in adolescents with major depressive and anxiety disordersMadelyn A Gillentine, Ricardo Lozoya, Jiani Yin, et al.
Scientific Reports|February 19, 2020
Exome Sequencing in Individuals with Isolated Biliary AtresiaRamakrishnan Rajagopalan, Ellen A Tsai, Christopher M Grochowski, et al.
Pageof 8

Showing results (1-10 of 72) with videos related to

Sort By:
Pageof 8
Genes|August 28, 2025
Structural Variants: Mechanisms, Mapping, and Interpretation in Human GeneticsShruti Pande, Moez Dawood, Christopher M Grochowski
Current Protocols|May 22, 2024
Validation of Single-Nucleotide Mosaic Variants Through Droplet Digital PCRChristopher M Grochowski, Richard A Gibbs, Harsha Doddapaneni
Gene|November 10, 2015
Jagged1 (JAG1): Structure, expression, and disease associationsChristopher M Grochowski, Kathleen M Loomes, Nancy B Spinner
Trends in Genetics : TIG|July 12, 2022
Complex genomic rearrangements: an underestimated cause of rare diseasesJakob Schuy, Christopher M Grochowski, Claudia M B Carvalho, et al.
Current Protocols in Human Genetics|March 17, 2020
Quantitative Assessment of Parental Somatic Mosaicism for Copy-Number Variant (CNV) DeletionsQian Liu, Christopher M Grochowski, Weimin Bi, et al.
Journal of Child and Adolescent Psychopharmacology|August 18, 2017
CHRNA7 Deletions are Enriched in Risperidone-Treated Children and AdolescentsMadelyn A Gillentine, Janson J White, Christopher M Grochowski, et al.
Biorxiv : the Preprint Server for Biology|February 14, 2024
Genome-wide maps of highly-similar intrachromosomal repeats that mediate ectopic recombination in three human genome assembliesLuis Fernandez-Luna, Carlos Aguilar-Perez, Christopher M Grochowski, et al.
HGG Advances|December 26, 2024
Genome-wide maps of highly-similar intrachromosomal repeats that can mediate ectopic recombination in three human genome assembliesLuis Fernandez-Luna, Carlos Aguilar-Perez, Christopher M Grochowski, et al.
Journal of Affective Disorders|July 21, 2018
CHRNA7 copy number gains are enriched in adolescents with major depressive and anxiety disordersMadelyn A Gillentine, Ricardo Lozoya, Jiani Yin, et al.
Scientific Reports|February 19, 2020
Exome Sequencing in Individuals with Isolated Biliary AtresiaRamakrishnan Rajagopalan, Ellen A Tsai, Christopher M Grochowski, et al.
Pageof 8